Cordis Corporation
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories4
Latest FDA decision2022-04-06
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220654 | ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire | NTE | 2022-04-06 | View |
| 510(k) | K212977 | SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands | DQO | 2022-02-17 | View |
| 510(k) | K210626 | SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter | LIT | 2021-04-23 | View |
| 510(k) | K202167 | Brite Tip Radianz Guiding Sheath | DYB | 2021-02-26 | View |
| 510(k) | K201377 | SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter | LIT | 2020-10-09 | View |
| 510(k) | K201333 | SABER .035 PTA Dilatation Catheter | LIT | 2020-09-11 | View |
| 510(k) | K181592 | RAIN Sheath Transradial | DYB | 2018-08-15 | View |
| 510(k) | K180081 | RAILWAY Sheathless Access System | DYB | 2018-04-18 | View |
No matching devices.